Cough Drops Freegells Strawberry 30ct

Manufacturer
RL Albert & Son Inc.
Effective date
2025-10-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:39:54

Label at a glance#

ProductCough Drops Freegells Strawberry 30ct
Active ingredientLEVOMENTHOL
Label structure7 sections

Indications and uses

temporarily relieves: cough as may occur with a cold occasional minor irritation and sore throat

Dosage and administration

 adults and children 5 years and over   dissolve 2 lozenge (one at time) slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor.  children under 5 years   ask a doctor 

Label contents#

Full prescribing information#

Active ingredient (in each drop)

OTC - ACTIVE INGREDIENT SECTION

Menthol 2.7 mg

Purpose

OTC - PURPOSE SECTION

Cough suppressant/Oral anesthetic

Uses

INDICATIONS & USAGE SECTION

  • temporarily relieves:
  • cough as may occur with a cold
  • occasional minor irritation and sore throat

Warnings

WARNINGS SECTION

Sore throat warning:if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. If sore mouth symptoms do not improve in 7 days, see your dentist or doctor promptly. These symptoms may be serious.

Ask a doctor before use if you have:

  • persistent or chronic cough such as occurs with smoking, asthma, or emphysema
  • cough accompanied by excessive phlegm (mucus)

Stop use and ask a doctor if

  • cough persists for more than 7 days, tends to recur, or is accompanied by fever, rash, or persistent headache, These could be signs of a serious condition.
  • sore throat is severe, or irritation, pain or redness lasts or worsens
  • sore mouth does not improve in 7 days

If pregnant or breast-feeding
ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

 adults and children 5 years and over  dissolve 2 lozenge (one at time) slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor.
 children under 5 years  ask a doctor 

Other information

SPL UNCLASSIFIED SECTION

  • 11 calories per drop
  • do not use if bags is torn or open
  • Contains: Soy

Inactive ingredients

INACTIVE INGREDIENT SECTION

Citric Acid, corn syrup, eucalyptus oil, FD&C red no. 40, natural & artificial flavoring, soy lecithin, sucrose and water.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83002-038-01Cough Drops Freegells Strawberry 30ct30 in 1 BAGLOZENGE302
83002-038-01Cough Drops Freegells Strawberry 30ct9 in 1 CARTONLOZENGE92

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83002-03883002-038-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12024-03-12full-release2026-06-01 00:09:47

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Cough Drops Freegells Strawberry 30ctMENTHOLRL Albert & Son Inc.2ea760f3-df50-4c46-a43d-d5ed07f421a52025-10-08WarningsExact identifier
ndc (package): 83002-038-01
ndc (product): 83002-038
ndc11 (package): 83002003801
spl id: 40ab7106-d489-021e-e063-6294a90a4869
spl set id: 2ea760f3-df50-4c46-a43d-d5ed07f421a5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.